SSF1 Polyclonal Antibody, 20ul Peptide Modification Mutations in this gene cause

Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM)

This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation

subcellular location:Predominantly on lateral parts of the membrane

ANGPTL4 encodes a glycosylated

SSF1 Polyclonal Antibody, 20ul Peptide Modification Mutations in this gene causeThe protein encoded by this gene is an evolutionarily conserved protein similar to yeast SSF1 as well as to the gene product of the Drosophila gene peter pan (ppan). SSF1 is known to be involved in the second step of mRNA splicing. Both SSF1 and ppan are essential for cell growth and proliferation. Exogenous expression of this gene was reported to reduce the anchorage independent growth of some tumor cells. Read through transcription of this gene with